Acetyl phosphate (BioCAD00000005775)

placenta

Metabolite Card

Formula: C2H5O5P (139.9875)
SMILES: CC(=O)OP(O)(O)=O

Synonyms [en]

ACETYL PHOSPHATE; acetylphosphate; Monoacetyl phosphate; (acetyloxy)phosphonic acid; acetyl dihydrogen phosphate; acetylphosphoric acid

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Acetyl phosphate. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000005775). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Acetylphosphate, also known as acetyl-p, belongs to the class of organic compounds known as acyl monophosphates. These are organic compounds containing a monophosphate linked to an acyl group. They have the general structure R-CO-P(O)(O)OH, R=H or organyl. Since acetylphosphate synthesis is known to depend on cholinesterase activity, pseudocholinesterase was assumed to participate to a small extent in acetylphosphate synthesis by cancerous serum. It is also an intermediate in pyruvate metabolism. Acetylphosphate is a drug. Acetylphosphate exists in all living organisms, ranging from bacteria to humans. Acetylphosphate can be converted into acetic acid; which is mediated by the enzyme acylphosphatase-1. It is generated from pyruvate and the formation is catalyzed by pyruvate oxidase (EC:1.2.3.3). In humans, acetylphosphate is involved in the metabolic disorder called the pyruvate dehydrogenase complex deficiency pathway. It is generated from sulfoacetaldehyde, converted to acetyl-CoA and acetate via phosphate acetyltransferase (EC:2.3.1.8) and acetate kinase (EC:2.7.2.1) respectively. Acetylphosphate or actyl phosphate is a compound involved in taurine and hypotaurine metabolism as well as pyruvate metabolism. Cancerous serum produced 37% less acetylphosphate than normal serum.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 590-54-5
  • PubChem: 186
  • ChEBI: ChEBI:15350
  • HMDB: HMDB0001494
  • KEGG: C00227
  • NCBI MeSH: acetyl phosphate
  • DrugBank: DB02897
  • RefMet: RM0136104
  • MoNA: BAF_UVA_POS001487
  • MoNA: EMBL_MCF_2_0_HRMS_Library000233
  • MoNA: HMDB0001494_ms_ms_1613
  • MoNA: HMDB0001494_ms_ms_1614
  • MoNA: HMDB0001494_ms_ms_1615
  • MoNA: MoNA038671
  • MoNA: PS010801
  • MoNA: PS010802
  • Metlin: METLIN_63131
  • Coconut NaturalProduct: CNP0284907.0

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R00207 1.2.3.3 pyruvate:oxygen 2-oxidoreductase (phosphorylating)
KEGG:R00230 2.3.1.8 acetyl-CoA:phosphate acetyltransferase
KEGG:R00315 2.7.2.1 ATP:acetate phosphotransferase
KEGG:R00317 3.6.1.7 acetyl phosphate phosphohydrolase
KEGG:R00320 2.7.2.12 diphosphate:acetate phosphotransferase
KEGG:R00761 4.1.2.22 D-fructose-6-phosphate D-erythrose-4-phosphate-lyase (adding phosphate; acetyl-phosphate-forming)
KEGG:R01620 2.3.1.32 acetyl-phosphate:L-lysine N6-acetyltransferase
KEGG:R01621 4.1.2.9 D-xylulose 5-phosphate D-glyceraldehyde-3-phosphate-lyase (adding phosphate; acetyl-phosphate-forming)
KEGG:R05651 2.3.3.15 acetyl-phosphate:sulfite S-acetyltransferase (acyl-phosphate hydrolysing, 2-oxoethyl-forming)
KEGG:R07226 1.21.4.2 acetyl-phosphate ammonia:thioredoxin disulfide oxidoreductase (glycine-forming)
KEGG:R07227 1.21.4.3 acetyl-phosphate methylamine:thioredoxin disulfide oxidoreductase (N-methylglycine-forming)
KEGG:R07228 1.21.4.4 acetyl-phosphate trimethylamine:thioredoxin disulfide oxidoreductase (N,N,N-trimethylglycine-forming)
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Organism Source

Taxonomy Source

  1. Escherichia coli [ncbi taxid: 562]
  2. Escherichia coli KO11 [ncbi taxid: ]
  3. Homo sapiens [ncbi taxid: 9606]
  4. Mus musculus [ncbi taxid: 10090]

Pathway Synthetic

pathway id name
PathBank:SMP0002102 Acetate Metabolism
PathBank:SMP0120726 Leigh Syndrome
PathBank:SMP0120842 Pyruvate Kinase Deficiency
PathBank:SMP0000334 Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
PathBank:SMP0087394 Pyruvate Metabolism
PathBank:SMP0063661 Pyruvate Metabolism
PathBank:SMP0120753 Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
PathBank:SMP0120841 Primary Hyperoxaluria II, PH2
PathBank:SMP0120531 Pyruvate Dehydrogenase Complex Deficiency
PathBank:SMP0000196 Leigh Syndrome
PathBank:SMP0000559 Pyruvate Kinase Deficiency
PathBank:SMP0087325 Pyruvate Metabolism
PathBank:SMP0087449 Pyruvate Metabolism
PathBank:SMP0120533 Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
PathBank:SMP0120622 Primary Hyperoxaluria II, PH2
PathBank:SMP0000212 Pyruvate Dehydrogenase Complex Deficiency
PathBank:SMP0087231 Pyruvate Metabolism
PathBank:SMP0120751 Pyruvate Dehydrogenase Complex Deficiency
PathBank:SMP0120506 Leigh Syndrome
PathBank:SMP0120623 Pyruvate Kinase Deficiency
View All Pathways